A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3178514



Internal ID22335035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:132160168..132160501hg38UCSC Ensembl
chr7:131844927..131845260hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14428201
SamplesHG00514
Known GenesPLXNA4
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3178514
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer